Disease: High density lipoprotein measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149269
ABCA1
9 104884840 intron variant A/G snv 0.41 3
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 4
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs7120078
APLNR
11 57239072 upstream gene variant A/G snv 1.5E-02 3
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs1943981
LOC105372112
18 49643445 intergenic variant A/G;T snv 0.74 3
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs7518440
ARNT
1 150818286 non coding transcript exon variant A/G;T snv 3
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs11571111
REN
1 204161105 intron variant C/A snv 5.0E-03 4
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs8039217
STARD9
15 42694939 intron variant C/A snv 4.1E-02 5
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs235216
TNFRSF1B
1 12209567 downstream gene variant C/A;G;T snv 3